Name

generalized dystonia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease generalized dystonia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

generalized dystonia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease generalized dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

generalized dystonia Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 24 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant torsion dystonia 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant torsion dystonia 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myoclonic dystonia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myoclonic dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile-onset dystonia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile-onset dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 25 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 6, torsion Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 6, torsion phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 5, Dopa-responsive type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 5, Dopa-responsive type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 3, torsion, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 3, torsion, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile Parkinsonism-dystonia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile Parkinsonism-dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinsonism-Dystonia, Infantile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinsonism-Dystonia, Infantile from the curated CTD Gene-Disease Associations dataset.

Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset.

Dystonia musculorum deformans type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia musculorum deformans type 2 from the curated CTD Gene-Disease Associations dataset.

Dystonia 13, Torsion Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia 13, Torsion from the curated CTD Gene-Disease Associations dataset.

Dystonia musculorum deformans type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia musculorum deformans type 1 from the curated CTD Gene-Disease Associations dataset.

Torsion dystonia 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Torsion dystonia 7 from the curated CTD Gene-Disease Associations dataset.

Dystonia 17, Torsion, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia 17, Torsion, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Dystonia 15, myoclonic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia 15, myoclonic from the curated CTD Gene-Disease Associations dataset.

LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY from the curated CTD Gene-Disease Associations dataset.

Dystonia 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia 12 from the curated CTD Gene-Disease Associations dataset.

Myoclonic dystonia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myoclonic dystonia from the curated CTD Gene-Disease Associations dataset.

Familial paroxysmal dystonia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial paroxysmal dystonia from the curated CTD Gene-Disease Associations dataset.

Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency from the curated CTD Gene-Disease Associations dataset.

Hypermanganesemia with Dystonia Polycythemia and Cirrhosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypermanganesemia with Dystonia Polycythemia and Cirrhosis from the curated CTD Gene-Disease Associations dataset.

Juvenile-onset dystonia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Juvenile-onset dystonia from the curated CTD Gene-Disease Associations dataset.

Dystonia 3, Torsion, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia 3, Torsion, X-Linked from the curated CTD Gene-Disease Associations dataset.

Dystonia 6, torsion Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia 6, torsion from the curated CTD Gene-Disease Associations dataset.

Dystonia, Dopa-responsive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia, Dopa-responsive from the curated CTD Gene-Disease Associations dataset.

Cervical Dystonia, Primary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cervical Dystonia, Primary from the curated CTD Gene-Disease Associations dataset.

Dystonia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia from the curated CTD Gene-Disease Associations dataset.

dystonia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease dystonia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

deafness dystonia syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease deafness dystonia syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

dystonia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease dystonia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

dystonia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cranio-facial dystonia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease cranio-facial dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

focal dystonia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease focal dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

deafness dystonia syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease deafness dystonia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

dystonia, primary torsion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonia, primary torsion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complex regional pain syndromes; dystonia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complex regional pain syndromes; dystonia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myoclonus dystonia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myoclonus dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystonia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

idiopathic torsion dystonia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease idiopathic torsion dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystonia, primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonia, primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome deletion; dystonia; myoclonus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome deletion; dystonia; myoclonus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cervical dystonia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cervical dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystonia, cervical Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonia, cervical in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystonia, focal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonia, focal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blepharospasm; dystonia; dystonic disorders; torticollis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blepharospasm; dystonia; dystonic disorders; torticollis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystonia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystonia, early onset primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonia, early onset primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

akathisia, drug-induced; dystonia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease akathisia, drug-induced; dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystonia; psychomotor disorders; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonia; psychomotor disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

focal dystonia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease focal dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystonia Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term dystonia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

dystoniaparkinsonism Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term dystoniaparkinsonism in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Musician's dystonia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Musician's dystonia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

craniofacial dystonia Gene Set

From HPO Gene-Disease Associations

genes associated with the craniofacial dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

limb dystonia Gene Set

From HPO Gene-Disease Associations

genes associated with the limb dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

axial dystonia Gene Set

From HPO Gene-Disease Associations

genes associated with the axial dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

oromandibular dystonia Gene Set

From HPO Gene-Disease Associations

genes associated with the oromandibular dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dystonia Gene Set

From HPO Gene-Disease Associations

genes associated with the dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal dystonia Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

laryngeal dystonia Gene Set

From HPO Gene-Disease Associations

genes associated with the laryngeal dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

torsion dystonia Gene Set

From HPO Gene-Disease Associations

genes associated with the torsion dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

focal dystonia Gene Set

From HPO Gene-Disease Associations

genes associated with the focal dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Dystonia Musculorum Deformans Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Dystonia Musculorum Deformans phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Dystonia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Dystonia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

dystonia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dystonia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dystonia 6, torsion Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 6, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-17, primary torsion Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-17, primary torsion phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-parkinsonism, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-parkinsonism, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia 4, torsion, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 4, torsion, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia 13, torsion Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 13, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-12 phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia 21 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia 24 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 24 phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia 25 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, primary cervical Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, primary cervical phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, myoclonic Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, myoclonic phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, dystonia, and cerebral hypomyelination Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, dystonia, and cerebral hypomyelination phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-1, torsion Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-1, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.

{dystonia-1, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {dystonia-1, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinsonism-dystonia, infantile Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinsonism-dystonia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-7, torsion Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-7, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-11, myoclonic Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-11, myoclonic phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, juvenile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-15, myoclonic Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-15, myoclonic phenotype from the curated OMIM Gene-Disease Associations dataset.

hypermanganesemia with dystonia, polycythemia, and cirrhosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermanganesemia with dystonia, polycythemia, and cirrhosis phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, dopa-responsive, due to sepiapterin reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, dopa-responsive, due to sepiapterin reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leukoencephalopathy with dystonia and motor neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with dystonia and motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, early-onset atypical, with myoclonic features Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, early-onset atypical, with myoclonic features phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, dopa-responsive, with or without hyperphenylalaninemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, dopa-responsive, with or without hyperphenylalaninemia phenotype from the curated OMIM Gene-Disease Associations dataset.

Congenital generalized lipodystrophy type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital generalized lipodystrophy type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thyrotropin-releasing hormone resistance, generalized Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thyrotropin-releasing hormone resistance, generalized phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lipodystrophy, congenital generalized, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lipodystrophy, congenital generalized, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thyroid hormone resistance, generalized, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thyroid hormone resistance, generalized, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized arterial calcification of infancy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized arterial calcification of infancy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thyroid hormone resistance, generalized, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thyroid hormone resistance, generalized, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized dominant dystrophic epidermolysis bullosa Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized dominant dystrophic epidermolysis bullosa phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy with febrile seizures plus 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy with febrile seizures plus 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pustular psoriasis, generalized Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pustular psoriasis, generalized phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy with febrile seizures plus, type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy with febrile seizures plus, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy with febrile seizures plus, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy with febrile seizures plus, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy with febrile seizures plus, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy with febrile seizures plus, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucocorticoid resistance, generalized Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucocorticoid resistance, generalized phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy and paroxysmal dyskinesia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, Generalized Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Generalized from the curated CTD Gene-Disease Associations dataset.

Thyroid Hormone Resistance, Generalized, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thyroid Hormone Resistance, Generalized, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Generalized Epilepsy With Febrile Seizures Plus, Type 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 6 from the curated CTD Gene-Disease Associations dataset.

Lipodystrophy, Congenital Generalized Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipodystrophy, Congenital Generalized from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Idiopathic Generalized Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Idiopathic Generalized from the curated CTD Gene-Disease Associations dataset.

Thyroid Hormone Resistance, Generalized, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thyroid Hormone Resistance, Generalized, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Generalized Epilepsy and Paroxysmal Dyskinesia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Generalized Epilepsy and Paroxysmal Dyskinesia from the curated CTD Gene-Disease Associations dataset.

Generalized Epilepsy With Febrile Seizures Plus, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 1 from the curated CTD Gene-Disease Associations dataset.

Generalized Epilepsy With Febrile Seizures Plus, Type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 3 from the curated CTD Gene-Disease Associations dataset.

Generalized Epilepsy With Febrile Seizures Plus, Type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 4 from the curated CTD Gene-Disease Associations dataset.

Hypertrichosis congenital generalized X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertrichosis congenital generalized X-linked from the curated CTD Gene-Disease Associations dataset.

Generalized Epilepsy With Febrile Seizures Plus, Type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 2 from the curated CTD Gene-Disease Associations dataset.

Lipodystrophy, Congenital Generalized, Type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipodystrophy, Congenital Generalized, Type 3 from the curated CTD Gene-Disease Associations dataset.

Lipodystrophy, Congenital Generalized, Type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipodystrophy, Congenital Generalized, Type 4 from the curated CTD Gene-Disease Associations dataset.

Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia from the curated CTD Gene-Disease Associations dataset.

congenital generalized lipodystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease congenital generalized lipodystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital generalized lipodystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease congenital generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

generalized atherosclerosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease generalized atherosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

epilepsy with generalized tonic-clonic seizures Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease epilepsy with generalized tonic-clonic seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

idiopathic generalized epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease idiopathic generalized epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

generalized epilepsy with febrile seizures plus Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease generalized epilepsy with febrile seizures plus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

generalized anxiety disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease generalized anxiety disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

glucose tolerance; lipids; atherosclerosis, generalized Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; lipids; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv; atherosclerosis, generalized Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis, generalized; vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis, generalized; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, generalized Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intima-media thickness; atherosclerosis, generalized Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intima-media thickness; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, absence; epilepsy, generalized Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, absence; epilepsy, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome deletion; epilepsy, generalized; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome deletion; epilepsy, generalized; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; atherosclerosis, generalized Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, generalized; epilepsy, reflex Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, generalized; epilepsy, reflex in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, generalized; seizures, febrile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, generalized; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis, generalized Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

generalized epilepsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease generalized epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, generalized; epilepsy, tonic-clonic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, generalized; epilepsy, tonic-clonic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

generalized epimerase-deficiency galactosemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease generalized epimerase-deficiency galactosemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, idiopathic generalized Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, idiopathic generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsies, partial; epilepsy, generalized; seizures, febrile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsies, partial; epilepsy, generalized; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipids; atherosclerosis, generalized Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipids; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

generalized Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term generalized in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Generalized seizures_Brain_GSE6614 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Generalized seizures_Brain_GSE6614 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Epilepsy (generalized) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Epilepsy (generalized) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

generalized hypotonia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the generalized hypotonia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

generalized amyloid deposition Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the generalized amyloid deposition phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

moderate generalized osteoporosis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the moderate generalized osteoporosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

generalized abnormality of skin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the generalized abnormality of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

generalized osteosclerosis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the generalized osteosclerosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

eeg with generalized epileptiform discharges Gene Set

From HPO Gene-Disease Associations

genes associated with the eeg with generalized epileptiform discharges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized osteosclerosis Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized osteosclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized limb muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized limb muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hyperreflexia Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hyperreflexia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized tonic seizures Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized tonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized abnormality of skin Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized bone demineralization Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized bone demineralization phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized morning stiffness Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized morning stiffness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized muscle hypertrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized muscle hypertrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized amyotrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized arterial tortuosity Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized arterial tortuosity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized opacification of the cornea Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized opacification of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hypotonia Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hyperpigmentation Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hyperpigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hirsutism Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hirsutism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hypopigmentation of hair Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hypopigmentation of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized aminoaciduria Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized aminoaciduria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized seborrheic dermatitis Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized seborrheic dermatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized myoclonic seizures Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized myoclonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized arterial calcification Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized arterial calcification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized edema Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

eeg with generalized slow activity Gene Set

From HPO Gene-Disease Associations

genes associated with the eeg with generalized slow activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intermittent generalized erythematous papular rash Gene Set

From HPO Gene-Disease Associations

genes associated with the intermittent generalized erythematous papular rash phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized tonic-clonic seizures Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized tonic-clonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized seizures Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized neonatal hypotonia Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized neonatal hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hyperkeratosis Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hyperkeratosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized osteoporosis with pathologic fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized osteoporosis with pathologic fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hypopigmentation Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hypopigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized papillary lesions Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized papillary lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hypotonia due to defect at the neuromuscular junction Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized distal tubular acidosis Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized distal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized cerebral atrophy/hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized clonic seizures Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized clonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized muscular appearance from birth Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized muscular appearance from birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized joint laxity Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized joint laxity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital, generalized hypertrichosis Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital, generalized hypertrichosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized lipodystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized lipodystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized amyloid deposition Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized amyloid deposition phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Epilepsy, Generalized Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Epilepsy, Generalized phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

epilepsy, idiopathic generalized, susceptibility to, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, idiopathic generalized, susceptibility to, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, 10} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, 10} phenotype from the curated OMIM Gene-Disease Associations dataset.

generalized epilepsy and paroxysmal dyskinesia Gene Set

From OMIM Gene-Disease Associations

genes associated with the generalized epilepsy and paroxysmal dyskinesia phenotype from the curated OMIM Gene-Disease Associations dataset.

epilespy, generalized, with febrile seizures plus, type 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilespy, generalized, with febrile seizures plus, type 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, susceptibility to, 9} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, suscpetibility to, 12} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, suscpetibility to, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.

generalized epilepsy with febrile seizures plus, type 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the generalized epilepsy with febrile seizures plus, type 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, generalized, with febrile seizures plus, type 5, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, generalized, with febrile seizures plus, type 5, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

thyrotropin-releasing hormone resistance, generalized Gene Set

From OMIM Gene-Disease Associations

genes associated with the thyrotropin-releasing hormone resistance, generalized phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, idiopathic generalized, susceptibility to 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, idiopathic generalized, susceptibility to 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, generalized, with febrile seizures plus, type 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, generalized, with febrile seizures plus, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, generalized, with febrile seizures plus, type 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, generalized, with febrile seizures plus, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, generalized, with febrile seizures plus, type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, generalized, with febrile seizures plus, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, generalized, with febrile seizures plus, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, generalized, with febrile seizures plus, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, generalized, with febrile seizures plus, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, generalized, with febrile seizures plus, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, generalized, with febrile seizures plus, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, generalized, with febrile seizures plus, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

?lipodystrophy, congenital generalized, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?lipodystrophy, congenital generalized, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

epidermolysis bullosa, generalized atrophic benign Gene Set

From OMIM Gene-Disease Associations

genes associated with the epidermolysis bullosa, generalized atrophic benign phenotype from the curated OMIM Gene-Disease Associations dataset.

lipodystrophy, congenital generalized, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lipodystrophy, congenital generalized, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertrichosis, congenital generalized Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypertrichosis, congenital generalized phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy idiopathic generalized, susceptibility to, 8} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy idiopathic generalized, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertrichosis terminalis, generalized, with or without gingival hyperplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypertrichosis terminalis, generalized, with or without gingival hyperplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

lipodystrophy, congenital generalized, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lipodystrophy, congenital generalized, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

lipodystrophy, congenital generalized, type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lipodystrophy, congenital generalized, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, susceptibility to, 11} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 11} phenotype from the curated OMIM Gene-Disease Associations dataset.

arterial calcification, generalized, of infancy, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arterial calcification, generalized, of infancy, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

arterial calcification, generalized, of infancy, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arterial calcification, generalized, of infancy, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.